2-(Methoxymethoxy)-4-(trifluoromethoxy)benzaldehyde
95%
- Product Code: 42045
CAS:
1321963-79-4
| Molecular Weight: | 250.17 g./mol | Molecular Formula: | C₁₀H₉F₃O₄ |
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| EC Number: | MDL Number: | MFCD27943593 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both methoxymethoxy and trifluoromethoxy groups, makes it valuable in the synthesis of pharmaceuticals and agrochemicals. It is often employed in the preparation of compounds with potential biological activity, particularly in the development of drugs targeting neurological disorders or as a building block for herbicides and pesticides. The trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting compounds, making it a preferred choice in medicinal chemistry. Additionally, it is used in research settings to explore novel chemical reactions and pathways due to its unique functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $41.85 |
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| 0.250 | 10-20 days | $75.07 |
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| 1.000 | 10-20 days | $288.93 |
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2-(Methoxymethoxy)-4-(trifluoromethoxy)benzaldehyde
This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both methoxymethoxy and trifluoromethoxy groups, makes it valuable in the synthesis of pharmaceuticals and agrochemicals. It is often employed in the preparation of compounds with potential biological activity, particularly in the development of drugs targeting neurological disorders or as a building block for herbicides and pesticides. The trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting compounds, making it a preferred choice in medicinal chemistry. Additionally, it is used in research settings to explore novel chemical reactions and pathways due to its unique functional groups.
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